The new National Institute of Health and Care Excellence (NICE) UK guideline for ME/CFS have just been published. Read more
The theme for this year's celebration is Millions of Reasons to Care. Most people who provide care don’t see themselves as carers, they instead see themselves as parents, partners, children, extended family members or friends. Read more
An important part of improving outcomes for people living with ME/CFS is educating healthcare professionals about the condition and what they can to do help. Read more
Module 2 of our GP Education program focuses on ensuring a patient-centered approach to care for people living with ME/CFS. Has your GP completed it yet? Read more
Emerge Australia's Online Community Groups program has launched two online peer support groups for family members and carers of people living with ME/CFS. Read more
Read an update and statement from Emerge Australia on the current delays on the UK's NICE clinical guidelines for ME/CFS. Read more
The CHROMIC study aims to improve the understanding of the disorder as well as to look for new treatments for ME/CFS. Click here to learn about how you can participate. Read more
In May, the US Centers for Disease Control and Prevention (CDC) released a draft of its evidence review on the diagnosis and treatment of ME/CFS for public comment. Read more
The ANCHOR study aims to the quality of life, social, educational and economic impacts of ME/CFS Read more